510(k) K073523 ยท NFA Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection
INTERCEPTOR PLUS CORONARY FILTER SYSTEMS
| Applicant | Medtronic, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Aug 1, 2008 |
| Received | Dec 14, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073523
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.